- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06389227
Developing the Physical Performance in Youth Soccer
April 30, 2024 updated by: University of Turin, Italy
Developing the Physical Performance in Youth Soccer: Short-term Effect of Dynamic-Ecological Versus Traditional Training Approach for Sub-élite U13 Players: An Ecological Exploratory Cluster Randomised Trial
Therefore, this study aims to verify the effects of a soccer training program based on the dynamic-ecological approach on U13 sub-elité players' physical efficiency by analysing explosive strength, speed, resistance to speed and muscle flexibility.
This study hypothe-sises that the dynamic-ecological approach can consistently help players develop adequate physical efficiency and motor coordination.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Nowadays, research in youth soccer consists of methodological choices that can raise ac-tivity volumes and exercise intensity to promote proper training for youth soccer de-mands.
Therefore, the present cluster randomised trial aims to evaluate the effects on physical performance parameters of the dynamic-ecological approach compared with a traditional one in a group of sub-élite U13 players.
Thirty-five male children (age 12.16 ± 0.55 years; weight 45.59 ± 7.15 kg; height 145.5 ± 4.2 cm; BMI 15.8 ± 2.1 kg*m-²) were re-cruited for this trial from two teams belonging to sub-élite soccer schools and randomly assigned in a dynamic-ecological approach (DEA) or a traditional training (TTG) group.
The training program lasted six weeks and consisted of 18 training sessions of 90 minutes each (3 sessions per week).
The sample was evaluated by Standing Long Jump (SLJ), hop test (HT), 10 m sprint (10m), 10 x 5 m shuttle run test (SRT) and Leg Raise test (LR).
The DEA group showed significantly higher results in the SLJ (p< .001),
HT left leg (p<.001),
10m sprint (p<.001),
and SRT (p<.001).
In conclusion, the dynamic-ecological approach provides higher performance adaptations.
Therefore, this approach can be considered a suitable method to optimise prepubertal player training, mainly when no fitness or strength coach is available.
Study Type
Interventional
Enrollment (Actual)
35
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Turin, Italy, 10100
- Cit Turin LDE
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- had not suffered an injury in the previous 6 months;
- who, in the 4 weeks before the study, had systematically performed the training sessions without interruptions or absences;
- all those who, upon medical evaluation, fell within stages 3 and 4 of Tanner's classification
Exclusion Criteria:
-Goalkeepers and players who had been injured in the previous six months or did not meet the established minimum compliance were excluded from this study
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: dynamic-ecological approach (DEA)
The DEA completed 18 ninety-minute sessions (3 per week) for six weeks oriented to soccer training using the dynamic ecological approach
|
The DEA completed 18 ninety-minute sessions (3 per week) for six weeks oriented to soccer training using the dynamic ecological approach
|
Active Comparator: traditional training group (TTG)
TTG followed a traditional soccer training program for the same period and number of ses-sions without any intervention attributable to the dynamic ecological approach
|
The TTG followed a traditional soccer training program for the same period and number of sessions without any intervention attributable to the dynamic ecological approach
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Number of participants evaluated on physical efficiency
Time Frame: From enrollment to the end of the study at six weeks
|
Direct outcome measurements pre-test vs post-test, Intervention vs treatment
|
From enrollment to the end of the study at six weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Federico Abate Daga, MSC PhD, University of Turin, Italy
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
October 15, 2023
Primary Completion (Actual)
October 30, 2023
Study Completion (Actual)
February 15, 2024
Study Registration Dates
First Submitted
April 24, 2024
First Submitted That Met QC Criteria
April 26, 2024
First Posted (Actual)
April 29, 2024
Study Record Updates
Last Update Posted (Estimated)
May 2, 2024
Last Update Submitted That Met QC Criteria
April 30, 2024
Last Verified
April 1, 2024
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 0433611
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
Italian GDPR law
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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